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Journal Abstract Search

336 related items for PubMed ID: 11518736

  • 1. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene.
    Montosi G, Donovan A, Totaro A, Garuti C, Pignatti E, Cassanelli S, Trenor CC, Gasparini P, Andrews NC, Pietrangelo A.
    J Clin Invest; 2001 Aug; 108(4):619-23. PubMed ID: 11518736
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  • 6. Non-HFE hemochromatosis.
    Pietrangelo A.
    Semin Liver Dis; 2005 Nov; 25(4):450-60. PubMed ID: 16315138
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  • 7. Genes that modify the hemochromatosis phenotype in mice.
    Levy JE, Montross LK, Andrews NC.
    J Clin Invest; 2000 May; 105(9):1209-16. PubMed ID: 10791995
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  • 9. Iron overload: molecular clues to its cause.
    Kühn LC.
    Trends Biochem Sci; 1999 May; 24(5):164-6. PubMed ID: 10322426
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  • 10. Genetic background of primary iron overload syndromes in Japan.
    Hayashi H, Wakusawa S, Motonishi S, Miyamoto K, Okada H, Inagaki Y, Ikeda T.
    Intern Med; 2006 May; 45(20):1107-11. PubMed ID: 17106152
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  • 12. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3).
    Devalia V, Carter K, Walker AP, Perkins SJ, Worwood M, May A, Dooley JS.
    Blood; 2002 Jul 15; 100(2):695-7. PubMed ID: 12091367
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  • 13. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M.
    Am J Hematol; 2006 Mar 15; 81(3):202-9. PubMed ID: 16493621
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  • 15. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr 15; 47(5):404-10. PubMed ID: 9510559
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  • 18. Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family.
    Rivard SR, Lanzara C, Grimard D, Carella M, Simard H, Ficarella R, Simard R, D'Adamo AP, De Braekeleer M, Gasparini P.
    Haematologica; 2003 Jul 15; 88(7):824-6. PubMed ID: 12857562
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  • 19. Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis.
    Muckenthaler M, Roy CN, Custodio AO, Miñana B, deGraaf J, Montross LK, Andrews NC, Hentze MW.
    Nat Genet; 2003 May 15; 34(1):102-7. PubMed ID: 12704390
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